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pubmed-article:7707521pubmed:abstractTextTo identify proteins involved in the formation of replication complexes at the 3' end of poliovirus negative-strand RNA, a combined in vitro biochemical and in vivo genetic approach was used. Five subgenomic cDNA constructs were generated to transcribe different negative-strand RNA fragments. In UV cross-linking assays, distinct differences in binding of proteins in extracts from poliovirus-infected and uninfected cells to virus-specific, radiolabeled transcripts were observed. Two proteins present in extracts from poliovirus-infected cells with approximate molecular masses of 36 and 38 kDa were shown to cross-link to the 3' end of poliovirus negative-strand RNA. Appearance of the 36- and 38-kDa proteins in UV cross-linking assays can be detected 3 to 3.5 h after infection, and cross-linking reaches maximum levels by 5 h after infection. The binding site for the 36-kDa protein overlaps with the computer-predicted loop b region of stem-loop I, the so-called cloverleaf structure, and the RNA sequence of this region is required for efficient binding. Transfection of full-length, positive-sense RNA containing a five-nucleotide substitution (positions 20 to 25) in the loop b region of stem-loop I into tissue culture cells yielded only viral isolates with a reversion at position 24 (U-->C). This finding demonstrates that the wild-type cytidine residue at position 24 is essential for virus replication. RNA binding studies with transcripts corresponding to the 3' end of negative-strand RNA suggest that complex formation with the 36-kDa protein plays an essential role during the viral life cycle.lld:pubmed
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pubmed-article:7707521pubmed:authorpubmed-author:SemlerB LBLlld:pubmed
pubmed-article:7707521pubmed:authorpubmed-author:RoehlH HHHlld:pubmed
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pubmed-article:7707521pubmed:articleTitlePoliovirus infection enhances the formation of two ribonucleoprotein complexes at the 3' end of viral negative-strand RNA.lld:pubmed
pubmed-article:7707521pubmed:affiliationDepartment of Microbiology and Molecular Genetics, College of Medicine, University of California, Irvine 92717, USA.lld:pubmed
pubmed-article:7707521pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:7707521pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:7707521pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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